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Metal–support interactions in Pt/Al2O3 and Pd/Al2O3 catalysts for CO oxidation

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TLDR
In this paper, the properties of the catalysts denoted as Pt(Pd)/Al2O3(X)-Y (X − calcination temperature of support, ǫ; Y − calcification temperature of catalyst,ǫ) were studied as a function of the temperatures used for calcination of the support and/or the catalyst in oxygen or in a reaction mixture of CO+O2.
Abstract
Platinum and palladium catalysts supported on γ-Al2O3 were studied by XRD, UV–vis DRS, HRTEM, TPR-H2, XPS together with measurements of their catalytic properties. The properties of the catalysts denoted as Pt(Pd)/Al2O3(X)-Y (X—the calcination temperature of support, °C; Y—the calcination temperature of catalyst, °C) were studied as a function of the temperatures used for calcination of the support and/or the catalyst in oxygen or in a reaction mixture of CO + O2. It was found that the deposition of Pt or Pd on γ-Al2O3 did not alter the structure of the support. Two types of the Pt and Pd particles were typically present on the γ-Al2O3 surface: individual particles with dimensions of 1.5–3 nm and agglomerates about 100 nm in size. In the catalysts calcined at relatively low temperatures (Pt/Al2O3(550)-450), platinum was present in the form of metal clusters. However, in the Pd/Al2O3(550)-450 catalyst, the palladium particles were almost completely decorated with a thin layer of an aluminate phase. These structures are not reduced in hydrogen in the temperature range of −15 to 450 °C, and are stable to treatment in a reaction mixture of CO + O2. Pd deposition on the γ-Al2O3-800 support was found to result in stabilization of the active component in two main forms, Pdo and PdO, with varying degrees of interaction due to the decoration effect. Calcination at the low temperature of 550 °C led to the formation of a so-called “core–shell structure”, where a palladium metal core is covered with a thin shell of an aluminate phase. Depending on the calcination temperature of the catalyst in the range of 450–1000 °C, the morphological form of the active component was converted from the “core-shell” state to a state consisting of two phases, Pdo and PdO, with a gradual decrease of the Pdo/PdO ratio, weakening the interaction with the support and the growth of palladium particles. Under the action of the reaction mixture, the Pd/Al2O3(800)-(450,600,800,1000) catalysts underwent changes in the Pdo/PdO ratio, which regulates the light-off temperature. After catalyst calcination at the highest temperature used in this study, 1200 °C, the palladium particles became much larger due to the loss of the palladium interaction with the support. Only the metal phase of palladium was observed in these catalysts, and their catalytic activity decreases substantially.

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Citations
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Journal ArticleDOI

Effect of Ceria Crystal Plane on the Physicochemical and Catalytic Properties of Pd/Ceria for CO and Propane Oxidation

TL;DR: In this article, the effects of ceria supports on physicochemical and catalytic properties of Pd/CeO2 for the CO and propane oxidation were examined, and the results showed that the structure and chemical state of pd on ceria were affected by ceria crystal planes.
Journal ArticleDOI

Continuous Hydrothermal Synthesis of Inorganic Nanoparticles: Applications and Future Directions

TL;DR: The state-of-art in the manufacture and applications of inorganic nanoparticles made using continuous hydrothermal flow synthesis (CHFS) processes are summarized, ideal requirements of any flow process for nanoceramics production are introduced, different approaches to CHFS are outlined, and the pertinent properties of supercritical water and issues around mixing in flow are introduced.
Journal ArticleDOI

Strong Metal-Support Interactions between Pt Single Atoms and TiO2.

TL;DR: It is demonstrated that the SMSI can occur on TiO 2 supported Pt single atoms but at a much higher reduction temperature than that on Pt nanoparticles (NPs) and revealed that in 3-nitrostyrene hydrogenation reaction single atoms are the real active sites while Pt NPs barely contribute to the activity through selectively encapsulating the NP sites.
Journal ArticleDOI

CO oxidation over graphene supported palladium catalyst

TL;DR: Graphene supported palladium (Pd) catalyst has been prepared using the conventional impregnation and hydrogen reduction method in this article, and the density functional theory (DFT) study and the catalyst characterization using Raman and X-ray photoelectron spectroscopy confirm that oxygen containing groups play an important role in stabilizing Pd clusters on graphene.
Journal ArticleDOI

Catalysis by gold: New insights into the support effect

TL;DR: In this article, the metal-support interaction (MSI) plays an essential role in the catalysis by gold and the catalytic mechanisms for low-temperature CO oxidation over RMO supported gold catalysts are discussed based on the recent progress on this topic.
References
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A case study: surface chemistry and surface structure of catalytic aluminas, as studied by vibrational spectroscopy of adsorbed species

TL;DR: The main attention has been devoted to various aspects of the surface chemistry of aluminas, as revealed by the adsorption of selected probe molecules, rather than to a systematic description of the very many probe molecules used over the years.
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